Variant #0013079631 (NC_000023.10:g.152988615G>A, NM_001256447.1:c.85C>T (BCAP31))

Chromosome X
Affects function (as reported) Not classified
Affects function (by curator) Not classified
DNA change (genomic) (Relative to hg19 / GRCh37) g.152988615G>A
DB-ID -
dbSNP ID rs782325268
gnomAD frequency 13/177657
gnomAD homozygote count 0/122029
Average frequency (gnomAD v.2.1.1) Retrieve
Database submission license No license selected
Created by LOVD
Date created 2017-02-27 00:00:00 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ABCD1 NM_000033.3 ./. c.-2107G>A r.(=) p.(=)
BCAP31 NM_001139441.1 ./. c.85C>T r.(?) p.(Pro29Ser)
BCAP31 NM_001139457.2 ./. c.286C>T r.(?) p.(Pro96Ser)
BCAP31 NM_001256447.1 ./. c.85C>T r.(?) p.(Pro29Ser)
BCAP31 NM_005745.7 ./. c.85C>T r.(?) p.(Pro29Ser)